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Facile Hydrogenative Deprotection of N-Benzyl Groups Using a Mixed Catalyst of Palladium and Niobic Acid-on-Carbon

[Image: see text] The palladium-on-carbon (Pd/C)-catalyzed hydrogenative deprotection of the N-benzyl-protecting group was effectively facilitated by the combined use of niobic acid-on-carbon (Nb(2)O(5)/C). Nb(2)O(5)/C is an acidic heterogeneous catalyst prepared from NbCl(5) and activated carbon. T...

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Detalles Bibliográficos
Autores principales: Yamamoto, Yuta, Shimizu, Eisho, Ban, Kazuho, Wada, Yoshiyuki, Mizusaki, Tomoteru, Yoshimura, Masatoshi, Takagi, Yukio, Sawama, Yoshinari, Sajiki, Hironao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033673/
https://www.ncbi.nlm.nih.gov/pubmed/32095693
http://dx.doi.org/10.1021/acsomega.9b03226
Descripción
Sumario:[Image: see text] The palladium-on-carbon (Pd/C)-catalyzed hydrogenative deprotection of the N-benzyl-protecting group was effectively facilitated by the combined use of niobic acid-on-carbon (Nb(2)O(5)/C). Nb(2)O(5)/C is an acidic heterogeneous catalyst prepared from NbCl(5) and activated carbon. The catalysts were easily removed from the reaction mixture and reusable. Deprotected amines were obtained in excellent yields without an additional neutralization process. The facilitating effect of Nb(2)O(5)/C was also observed during the Pd/C-catalyzed hydrogenative deprotection of the N-benzyloxycarbonyl (Cbz) and O-benzyl groups.